Investment Rating - The report maintains a "Buy" rating for the company [4][6]. Core Insights - The company achieved a revenue of 23.188 billion yuan in the first three quarters of 2025, representing a year-on-year increase of 14.85%. The net profit attributable to the parent company was 5.751 billion yuan, up 24.50%, and the net profit after deducting non-recurring gains and losses was 5.589 billion yuan, an increase of 21.08% [1][4][6]. Summary by Sections Internationalization and Partnerships - In Q3 2025, the company secured three overseas licensing agreements, including a collaboration with GSK to develop up to 12 innovative drugs, receiving an upfront payment of 500 million USD, with potential total payments of approximately 12 billion USD [2]. - The company also entered into a New-Co transaction with Braveheart Bio for HRS-1893, receiving an upfront payment of 65 million USD and potential milestone payments of up to 1.013 billion USD [2]. - Additionally, the company licensed part of its international market rights for a drug to Glenmark, receiving an upfront payment of 18 million USD and potential milestone payments of up to 1.093 billion USD [2]. Innovation and R&D - The company increased its R&D expenditure to 4.945 billion yuan in the first three quarters of 2025. New products were approved for market, including EZH2 inhibitors and a new oral hypoglycemic combination [3]. - The company has over 100 self-developed innovative products in clinical development and more than 400 clinical trials ongoing domestically and internationally [3]. - At the 2025 ESMO annual meeting, the company presented 46 research results in the oncology field, with significant findings published in The Lancet [3]. Financial Forecast - The company is projected to achieve net profits of 8.803 billion yuan, 10.277 billion yuan, and 12.151 billion yuan for 2025, 2026, and 2027, respectively, with year-on-year growth rates of 38.9%, 16.8%, and 18.2% [4][10].

Investment Rating - The report maintains a "Buy" rating for the company, indicating an expected price increase of over 15% in the next 6-12 months [5]. Core Insights - The company achieved a revenue of 15.76 billion RMB in H1 2025, representing a year-on-year growth of 15.88%, and a net profit attributable to shareholders of 4.45 billion RMB, up 29.67% year-on-year [2]. - The sales and licensing revenue from innovative drugs reached 9.56 billion RMB, accounting for 60.66% of total revenue, with significant contributions from new drugs such as Rivaroxaban and others [3]. - The company has successfully established multiple partnerships, generating substantial upfront payments, which have significantly enhanced its performance [3]. - R&D investment totaled 3.87 billion RMB in H1 2025, with a focus on over 100 innovative products undergoing more than 400 clinical trials [4]. - The company is expected to achieve revenues of 33.8 billion RMB, 38 billion RMB, and 42.6 billion RMB in 2025, 2026, and 2027 respectively, with net profits projected at 9 billion RMB, 10.5 billion RMB, and 12.1 billion RMB for the same years [5]. Summary by Sections Performance Review - In H1 2025, the company reported a revenue of 15.76 billion RMB, a 15.88% increase year-on-year, and a net profit of 4.45 billion RMB, reflecting a 29.67% growth [2]. Operational Analysis - The innovative drug sales and licensing revenue reached 9.56 billion RMB, with new drugs like Rivaroxaban and others showing strong growth [3]. - The company has successfully executed several high-value partnerships, including a 2 billion USD deal with MSD and a 750 million USD deal with IDEAYA, contributing to its revenue growth [3]. Research and Development - The company invested 3.87 billion RMB in R&D in H1 2025, with 6 new class 1 drugs approved, indicating a fruitful R&D phase [4]. - The company is conducting over 400 clinical trials for more than 100 innovative products, showcasing its commitment to innovation [4]. Profit Forecast and Valuation - The company is projected to achieve revenues of 33.8 billion RMB, 38 billion RMB, and 42.6 billion RMB in 2025, 2026, and 2027, respectively, with net profits expected to reach 9 billion RMB, 10.5 billion RMB, and 12.1 billion RMB [5].

香港交易及結算所有限公司及香港聯合交易所有限公司對本公告的內容概不負責，對其準確性 或完整性亦不發表任何聲明，並明確表示概不就因本公告全部或任何部分內容所產生或因依賴 該等內容而引致的任何損失承擔任何責任。 Jiangsu Hengrui Pharmaceuticals Co., Ltd. 江蘇恒瑞醫藥股份有限公司 （於中華人民共和國註冊成立的股份有限公司） （股份代號：1276） 海外監管公告 本公告乃根據香港聯合交易所有限公司證券上市規則第13.10B條刊發。 根據中華人民共和國的有關法例規定，江蘇恒瑞醫藥股份有限公司（「本公司」）在 上海證券交易所網站( www.sse.com.cn )刊發了以下公告。茲載列如下，僅供參閱。 承董事會命 江蘇恒瑞醫藥股份有限公司 董事長 孫飄揚先生 中國上海 2025年8月20日 於本公告日期，董事會成員包括(i)執行董事孫飄揚先生、戴洪斌先生、馮佶女 士、張連山先生、江寧軍先生及孫杰平先生；(ii)非執行董事郭叢照女士；及(iii) 獨立非執行董事董家鴻先生、曾慶生先生、孫金雲先生及周紀恩先生。 江苏恒瑞医药股份有限公司 2025 年半年度报告 公司代码：600276 ...

Core Insights - The National Medical Products Administration (NMPA) approved 43 new class 1 innovative drugs in the first half of 2025, a 59% increase year-on-year, nearing the total of 48 approvals for the entire year of 2024 [1] - The approval of innovative drugs is accelerating, with expectations for a record high in 2025 [1] Drug Type Distribution - Chemical drugs lead with 24 varieties, accounting for 56% of approvals; biological products follow with 14 varieties (32%); and traditional Chinese medicine and natural products account for 5 varieties (12%) [2] - The industry is transitioning from a "single-pole dominance" to a "multi-polar balance" [2] Therapeutic Area Insights - Oncology drugs dominate with 20 varieties, making up 47% of approvals; anti-infective drugs, traditional Chinese medicine, and endocrine/metabolic drugs each have 5 varieties (12%) [2] - The approval landscape shows a diverse range of therapeutic areas, with notable mentions for rare diseases and pediatric drugs [3] Review and Approval Process - 17 new drugs, approximately 40% of the total, received breakthrough therapy designation, including 8 biological products and 8 chemical drugs [2] - The NMPA is prioritizing the development of drugs for rare diseases and pediatric use, with specific plans in place for expedited review [3] Policy Support for Innovation - China's pharmaceutical innovation is rapidly advancing, with the country holding about 25% of the global innovative drug pipeline [4] - Recent policy measures, such as the implementation of the "Full Chain Support for Innovative Drug Development" plan, have significantly improved the speed of new drug inclusion in medical insurance [4] Future Initiatives - The NMPA plans to implement further measures to support innovative drug development, focusing on clinically valuable products and global synchronization of research [5] - Efforts will include optimizing review processes, enhancing intellectual property protections, and aligning with international standards to facilitate global competitiveness [5]

Investment Rating - The report indicates a positive investment rating for the innovative drug sector, particularly highlighting the success of the combination therapy of Bemesumab and Anlotinib in treating NSCLC [8][11]. Core Insights - The report emphasizes the significant progress in the treatment of non-small cell lung cancer (NSCLC) through innovative therapies, particularly the combination of immune checkpoint inhibitors and anti-angiogenic agents, which have shown improved progression-free survival (PFS) rates compared to traditional therapies [7][11]. - The CAMPASS trial demonstrated that the combination of Bemesumab and Anlotinib significantly extended the median PFS to 11.0 months compared to 7.1 months for the control group, marking a notable advancement in first-line treatment options for PD-L1 positive advanced NSCLC [11]. - The report also discusses the ongoing clinical trials and the potential for new drug approvals, indicating a robust pipeline for innovative therapies in the oncology sector [12][47]. Summary by Sections Section 1: Focus on Innovative Drugs - The report reviews the latest developments in innovative drugs, particularly in the context of NSCLC treatments and highlights the importance of combination therapies [2][3]. Section 2: Clinical Trial Results - The report details the results of the CAMPASS trial, which compared the efficacy of Bemesumab combined with Anlotinib against Pembrolizumab in treating advanced NSCLC, showcasing a significant improvement in PFS [11][12]. - It also covers the mid-term analysis of the TQB2450-III-12 trial, which further supports the efficacy of the Bemesumab and Anlotinib combination in squamous NSCLC [13]. Section 3: Market Developments - The report notes the recent approvals and submissions for new drug indications, reflecting a dynamic and rapidly evolving market for innovative cancer therapies [45][49]. - It highlights the performance of various biotech companies in the market, indicating significant fluctuations in stock prices and market capitalization [41][43].

Investment Rating - The report maintains an "Accumulate" rating for the pharmaceutical and biotechnology industry [1]. Core Insights - The stroke treatment market in China is projected to exceed 100 billion yuan, with QHRD106 from Qianhong Pharmaceutical expected to become a major product with potential sales of 4-5 billion yuan [1][19]. - The A-share pharmaceutical index has shown a year-to-date increase of 6.6%, outperforming the CSI 300 index by 9.0% [4][9]. - The report highlights the importance of secondary prevention in acute ischemic stroke (AIS) treatment, emphasizing the need for effective therapies [18][19]. Summary by Sections Industry Trends - The A-share pharmaceutical index has increased by 2.6% this week, with significant gains in various sub-sectors, including chemical drugs (+4.4%) and raw materials (+3.2%) [4][9]. - The H-share biotechnology index has shown a year-to-date increase of 41.4%, outperforming the Hang Seng Technology Index [4][9]. Market Potential - The number of stroke patients in China is approximately 13 million, with an annual increase of about 4.5%-4.8%, indicating a growing market for stroke medications [19][27]. - The report estimates that the sales peak for QHRD106 could reach 4-5 billion yuan by 2027, positioning it as a potential blockbuster drug [1][19]. R&D Progress and Company Dynamics - QHRD106 is currently in clinical phase II, with data expected to be released in the second half of 2025, potentially outperforming existing similar drugs [1][19]. - The report lists several companies to watch, including Qianhong Pharmaceutical, Hengrui Medicine, and BeiGene, focusing on growth potential in the innovative drug sector [10][11]. Investment Strategy - Recommended sub-sector rankings for investment are: innovative drugs > CXO > traditional Chinese medicine > medical devices > pharmacies > pharmaceutical commerce [10]. - Specific stock selection strategies include focusing on growth in innovative drugs and identifying undervalued stocks in traditional Chinese medicine [10].

Core Insights - A new Chinese innovative drug combination, "Defu Combination," has outperformed the global leader, Pembrolizumab (K drug), in treating PD-L1 positive advanced non-small cell lung cancer (NSCLC) [2][3] - The results were presented at the 2025 American Society of Clinical Oncology (ASCO) annual meeting, showcasing significant improvements in median progression-free survival (PFS) [2][4] Company Insights - China National Pharmaceutical Group (HK01177) reported that the "Defu Combination" achieved a median PFS of 11 months, surpassing K drug by 3.9 months, with a 30% reduction in the risk of disease progression or death [4] - The "Defu Combination" consists of two first-class innovative drugs: Anlotinib, a multi-targeted anti-angiogenic TKI approved in May 2018, and Bemarituzumab, a PD-L1 monoclonal antibody approved in May 2024 [3][4] Industry Insights - The CAMPASS study, a randomized controlled phase III trial, included 531 PD-L1 positive patients and demonstrated that the "Defu Combination" significantly benefits nearly all subgroups, especially those with high PD-L1 expression (TPS≥50%) [3][4] - The trend of increasing head-to-head clinical trials in China is notable, with domestic companies challenging established drugs like K drug, indicating a competitive landscape for innovative therapies [5][6] - The number of head-to-head trials initiated by domestic companies has risen from 2 in 2020 to 8 in 2023, reflecting a growing commitment to developing competitive treatments [6]